Table 1.
Analyte | MOF | Detection Limit | Water Stability | Detection Mechanism | Ref |
---|---|---|---|---|---|
CO2 | [Zn7(ip)12](OH)2 | - | High | QD | [27] |
UiO-66-ONa | 3.5 × 10−7 M | High | QD | [28] | |
H2S | UiO-66@NH2 | 118 μM | High | Target-mediated azide to amine reduction | [37] |
UiO-66@NO2 | 188 μM | High | Target-mediated nitro group to amine reduction | [38] | |
Zn-MOF | 28.3 μM | High | Target-mediated nitro group to amine reduction | [39] | |
Azide functionalized Ce-MOFs Nitro functionalized Ce-MOFs |
12.2 μM 34.8 μM |
High | Target-mediated azide/nitro groups to amine reduction | [40] | |
Al(OH)(IPA-N3) | 2.65 μM | High | Target-mediated N3 to amine reduction | [41] | |
Zr6O4(OH)4((NDC-(NO2)2)6 | 20 μM | High | Target-mediated nitro group to amine reduction | [42] | |
Al(OH)(BDC-N3) | 90.47 nM | High | Target-mediated N3 to amine reduction | [43] | |
Zr6O4(OH)4(BDC- (NO2)2)6 |
14.14 μM | High | Target-mediated nitro group to amine reduction | [44] | |
Eu3+/Cu2+@UiO-66- (COOH)2 |
- | High | Quench the broad LC emission through its superior affinity for Cu2+ ions | [47] | |
Eu3+/Ag+@UiO-66- (COOH)2 |
23.53 μM | High | - | [48] | |
UiO-66-MA | 3.3 nM | High | Michael addition to H2S | [49] | |
SO2 | MOF-5-NH2 | 0.168 ppm | High | - | [52] |
NO | Cu-TCA Eu-TCA |
0.1 mM 140 μM |
High | Cu2+ ions quench the ligand-based fluorescence Formation of coordination bonds between the europium and NO |
[58] |
UiO-66@NH2 | 0.575 μM | High | - | [59] | |
NO2 | {[Tb2(NBDC)3(DMF)4]·2DMF} {[Eu2(NBDC)3(DMF)4]·2DMF} |
1.8 ppm 2.2 ppm |
High | QD | [61] |
Fe2IIIMII, M = Co, Mn, and Zn | 500 ppb | High | QD | [62] | |
NH3 | Mg(H2DHBDC) Zn2(TCPE) |
- | High | FRET | [66] |
Eu3-functionalization MOF | 2.4 ppm | High | PET | [67] | |
(Zn2(bpdc)2(bpee) | 50 ppm | High | FRET | [68] |